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rs10227893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs10227893(G;G)
Make rs10227893(G;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position114630022
GeneFOXP2
is asnp
is mentioned by
dbSNPrs10227893
ebirs10227893
HLIrs10227893
Exacrs10227893
Varsomers10227893
Maprs10227893
PheGenIrs10227893
hapmaprs10227893
1000 genomesrs10227893
hgdprs10227893
ensemblrs10227893
gopubmedrs10227893
geneviewrs10227893
scholarrs10227893
googlers10227893
pharmgkbrs10227893
gwascentralrs10227893
openSNPrs10227893
23andMers10227893
23andMe allrs10227893
SNP Nexus

SNPshotrs10227893
SNPdbers10227893
MSV3drs10227893
GWAS Ctlgrs10227893
GMAF0.118
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[PMID 15877281OA-icon.png] variations in rs17137124 and rs10227893 may impair speech


ClinVar
Risk rs10227893(A,G;A,G)
Alt rs10227893(A,G;A,G)
Reference rs10227893(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene FOXP2
CLNDBN not specified
Reversed 0
HGVS NC_000007.13:g.114270077T>G
CLNSRC ClinVar
CLNACC RCV000081645.4,